chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5171529388171529389GT31GENIChomozygous55839482
5171529553171529554AAGGGGCCTGTCG32GENIChomozygous55839483
5171530403171530404TTC11GENICpossibly homozygous55839484
5171530431171530432A-18GENIChomozygous55839485
5171530531171530541AAAAAAAAAA----------5GENICheterozygous56619782
5171535441171535442CT24GENIChomozygous55839486
5171536009171536010CCAA9GENICpossibly homozygous55839487
5171536009171536010CCA9GENICheterozygous55839488
5171536467171536470TTT---14GENIChomozygous55839490
5171536474171536475TG16GENIChomozygous55948661
5171536527171536528AG20GENIChomozygous55839491
5171537585171537586TG25GENIChomozygous55839492
5171538208171538209AAT16GENIChomozygous55839493
5171539664171539665GC21GENIChomozygous55839494
5171539748171539749AG30GENIChomozygous55839495
5171540454171540455TG31GENIChomozygous55839496
5171540913171540914CT21GENICpossibly homozygous55839497
5171541733171541734AG32GENIChomozygous55839498
5171541738171541739TA31GENIChomozygous55839499